Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: < 0.01 (C)
Location

Chromosome 12:6355286 (forward strand)|View in location tab

Co-located variant

COSMIC COSM1179185

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB NM_001038.5:c.1129A>G

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 13 transcripts, has 2504 sample genotypes and is associated with 1 phenotype.

Variant displays